Pituitary I Flashcards

1
Q

What size are microadenomas and macroadenomas?

A

Microadenoma <= 1cm

Macroadenoma >1cm

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2
Q

What can a non-functioning pituitary adenoma cause?

A

Compression of optic chiasm and other structures, hypoadrenalism, hypothyroidism, hypogonadism, diabetes insipidus, GH deficiency

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3
Q

How are non-functioning pituitary adenomas managed?

A

Transsphenoidal surgery, replace hormones

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4
Q

What are physiological causes of raised prolactin?

A

Breast feeding, pregnancy, sleep, stress

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5
Q

What drugs can cause raised prolactin?

A

Dopamine antagonists, antipsychotics, antidepressants, oestrogen, cocaine

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6
Q

What are some pathologies that cause raised prolactin?

A

Hypothyroidism, stalk lesions, prolactinoma

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7
Q

What are the symptoms of a prolactinoma in a female?

A

Early presentation, galactorrhoea, menstrual irregularity, amenorrhoea, infertility

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8
Q

What are the symptoms of a prolactinoma in a male?

A

Late presentation, impotence, visual field abnormalities, headache, anterior pituitary malfunction

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9
Q

What investigations can be done for prolactinomas?

A

Serum prolactin concentration (raised)
MRI = micro/macroprolactinoma, pituitary stalk, optic chiasm
Visual fields = bilateral hemianopia
Pituitary function tests

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10
Q

What drug can be used to treat prolactinomas?

A

Dopamine antagonists = bromocriptine (3x daily orally), quinagolide (once daily orally), cabergoline (usually used, least side effects, once/twice week orally)

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11
Q

How successful are dopamine agonists in treating prolactinomas?

A

Very = prolactin normalised in 96%, menstruation regained in 94%, pregnancy rate 91%, tumour shrinkage

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12
Q

What are the side effects of prolactinomas?

A

Nausea/vomiting, low mood, fibrosis (heart valves/retroperitoneal)

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13
Q

What causes acromegaly?

A

Excess GH

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14
Q

What are the features of acromegaly?

A

Giant, thickened soft tissue (large jaw and hands), sweaty, snoring/sleep apnoea, hypertension, cardiac failure, headaches, diabetes, visual field abnormalities, hypopituitarism, early CV death, colonic polyps/cancer

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15
Q

How is acromegaly diagnosed?

A

IGF-1 = age and sex matched
GTT = suppression test, 75g oral then check GH at 0/30/60/90/120mins (GH unchanged, paradoxical rise)
Visual field and pituitary function tests
CT or MRI pituitary scan

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16
Q

How successful is surgery in treating acromegaly?

A

90% cure if microadenoma, 50% cure if macroadenoma

17
Q

How successful is radiotherapy alone in treating acromegaly?

A

25% success at three years

18
Q

What drugs can be used to treat acromegaly?

A

Somatostatin analogues = sandostatin LAR, lanreotide
Dopamine agonists = cabergoline
Pegvisomat = GH antagonist

19
Q

What are some features of somatostatin analogues used to treat acromegaly?

A

Reduces GH in most patients

Tumour shrinkage = 30-50% decrease in size, takes 6-12 months, re-expansion 6 weeks after stopping

20
Q

How are somatostatin analogues used to treat acromegaly pre-operatively?

A

Relieves headaches within 1hr, improves outcomes

21
Q

What are some side effects of somatostatin analogues?

A

Local stinging, flatulence, diarrhoea, abdominal pains, gallstones (60%, occur by 6 months, risk of biliary colic)

22
Q

What is the dosage of somatostatin analogues when treating acromegaly?

A

Sandostatin LAR = 10-30mg/28 days IM
Lanreotide autogel = 60-12-mg/28days SC
Pasireotide LAR = 40-60mg/28days IM

23
Q

What are some features of dopamine agonists used to treat acromegaly?

A

Cabergoline up to 3g weekly, work in around 10-15%, better if co-secreting prolactin

24
Q

What are some features of pegvisomat used to treat acromegaly?

A

SC injection 10-30mg daily, 85% response rate, tumour size doesn’t decrease, IGF-1 decreases but serum GH increases, last line treatment

25
Q

What must be managed in patients with acromegaly?

A

Cancer surveillance = colon and tubo-villous adenoma

CV risk factor management